Late-onset cobalamin C disease presenting with acute cerebellar ataxia

被引:0
作者
Yanping Wei
Honglin Hao
机构
[1] Chinese Academy of Medical Sciences and Peking Union Medical College,Department of Neurology, Peking Union Medical College Hospital
来源
Neurological Sciences | 2021年 / 42卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:4839 / 4842
页数:3
相关论文
共 54 条
[1]  
Carrillo-carrasco N(2012)Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management J Inherit Metab Dis 35 91-102
[2]  
Chandler RJ(2016)Acute ataxia in children: a review of the differential diagnosis and evaluation in the emergency department Pediatr Neurol 65 14-30
[3]  
Venditti CP(2006)Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12 Mol Genet Metab 88 138-145
[4]  
Caffarelli M(2019)Clinical feature and outcome of late-onset cobalamin C disease patients with neuropsychiatric presentations: a Chinese case series Neuropsychiatr Dis Treat 15 549-555
[5]  
Kimia AA(2018)Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations Metab Brain Dis 33 829-835
[6]  
Torres AR(2015)Clinical analysis of late-onset methylmalonic acidaemia and homocystinuria, cblC type with a neuropsychiatric presentation J Neurol Neurosurg Psychiatry 86 472-475
[7]  
Smith SE(2012)A clinical and gene analysis of late-onset combined methylmalonic aciduria and homocystinuria, cblC type China. J Neurol Sci 318 155-159
[8]  
Kinney HC(2014)Cobalamin C deficiency in an adolescent with altered mental status and anorexia Pediatrics 134 e1709-e1714
[9]  
Swoboda KJ(2006)Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations Mol Genet Metab 88 315-321
[10]  
Levy HL(2019)Distinct clinical, neuroimaging and genetic profiles of late-onset cobalamin C defects (cb1C): a report of 16 Chinese cases Orphanet J Rare Dis 14 109-7